TY - JOUR
T1 - Nonadiabatic Forward Flux Sampling for Excited-State Rare Events
AU - Reiner, Madlen Maria
AU - Bachmair, Brigitta
AU - Tiefenbacher, Maximilian Xaver
AU - Mai, Sebastian
AU - González, Leticia
AU - Marquetand, Philipp
AU - Dellago, Christoph
N1 - Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society.
PY - 2023/3/28
Y1 - 2023/3/28
N2 - We present a rare event sampling scheme applicable to coupled electronic excited states. In particular, we extend the forward flux sampling (FFS) method for rare event sampling to a nonadiabatic version (NAFFS) that uses the trajectory surface hopping (TSH) method for nonadiabatic dynamics. NAFFS is applied to two dynamically relevant excited-state models that feature an avoided crossing and a conical intersection with tunable parameters. We investigate how nonadiabatic couplings, temperature, and reaction barriers affect transition rate constants in regimes that cannot be otherwise obtained with plain, traditional TSH. The comparison with reference brute-force TSH simulations for limiting cases of rareness shows that NAFFS can be several orders of magnitude cheaper than conventional TSH and thus represents a conceptually novel tool to extend excited-state dynamics to time scales that are able to capture rare nonadiabatic events.
AB - We present a rare event sampling scheme applicable to coupled electronic excited states. In particular, we extend the forward flux sampling (FFS) method for rare event sampling to a nonadiabatic version (NAFFS) that uses the trajectory surface hopping (TSH) method for nonadiabatic dynamics. NAFFS is applied to two dynamically relevant excited-state models that feature an avoided crossing and a conical intersection with tunable parameters. We investigate how nonadiabatic couplings, temperature, and reaction barriers affect transition rate constants in regimes that cannot be otherwise obtained with plain, traditional TSH. The comparison with reference brute-force TSH simulations for limiting cases of rareness shows that NAFFS can be several orders of magnitude cheaper than conventional TSH and thus represents a conceptually novel tool to extend excited-state dynamics to time scales that are able to capture rare nonadiabatic events.
UR - http://www.scopus.com/inward/record.url?scp=85149471850&partnerID=8YFLogxK
U2 - 10.1021/acs.jctc.2c01088
DO - 10.1021/acs.jctc.2c01088
M3 - Article
AN - SCOPUS:85149471850
SN - 1549-9618
VL - 19
SP - 1657
EP - 1671
JO - Journal of Chemical Theory and Computation
JF - Journal of Chemical Theory and Computation
IS - 6
ER -